| NDC Code | 52959-730-21 |
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| Package Description | 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52959-730-21) |
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| Product NDC | 52959-730 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ciprofloxacin |
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| Non-Proprietary Name | Ciprofloxacin Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20040609 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA076794 |
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| Manufacturer | H.J. Harkins Company, Inc. |
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| Substance Name | CIPROFLOXACIN HYDROCHLORIDE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Quinolone Antimicrobial [EPC],Quinolones [CS] |
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